Food & Beverages
HIGH
FDA FOOD
Pacific Coast Producers Fruit Cocktail Recalled for Lead Contamination in 15 oz Cans (609 cases)
Potential contamination with heavy metal (Lead).
Pacific Coast Producers
Potential contamination
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
4,262 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 4,262
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Producers Pears Halves in Pear Juice Recall 2025 for Lead Contamination
Potential contamination with heavy metal (Lead).
Pacific Coast Producers
Potential contamination
Food & Beverages
HIGH
FDA FOOD
Gospodarstwo Pasieczne Sadecki Bartnik Bee Pollen 200g Recall for Pyrrolizidine Alkaloids (2025)
Gospodarstwo Pasieczne Sadecki Bartnik
detectable pyrrolizidine
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Producers Pears Sliced in Organic Pear Juice Recall 203 Cases for Lead Contamination (
Potential contamination with heavy metal (Lead).
Pacific Coast Producers
Potential contamination
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems IHDC30R D AND C PACK Medical Kits Recalled Over Re-Gassing (32,433 Units,
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Labor Delivery Packs Recalled for Re-Gassed Sterilization Flaw (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Medical Convenience Kits Over Re-Gassing Risk (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems High-Index Medical Kits Recalled for Re-Gassing After EO Sterilization Non
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems High-Rire Recall: 32,433 Medical Convenience Kits Recalled for Re-GassedEO
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
Lutronic XERF EFFECTOR 60 Electrosurgical Unit Recalled for Manufacturing Defects (2025-2026 Models)
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.
Lutronic
Manufacturing defects
Food & Beverages
HIGH
FDA FOOD
Organicare Nature's Science FemiClear Daily Bladder Strength Recall 15,075 Bottles in 2025 Over E. C
Microbial contamination with Escherichia coli O7:K1 and E. Coli 1303.
Organicare Nature's Science
Microbial contamination
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Medical Convenience Kits Recalled for Re-Gassing Risk
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalling 32,433 UDPG88W PICC G-TUBE Pack in 2025 Recall
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Medical Convenience Kits Over EO Re-Gassing Risk (2025)
American Contract Systems
Identified products
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Producers Halved Pears in Pear Juice Recall 2025 — 102 Cases Lead Contamination
Potential contamination with heavy metal (Lead).
Pacific Coast Producers
Potential contamination
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Angio Packs Over Re-Gassed EO Sterilization (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls 1 Allura Xper FD20/15 OR Table for Movement Failure Risk (2025)
Philips
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10/10 Recall for 286 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 OR Table Recall for 2 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DRUG
Sun Pharmaceutical Radiopharmaceutical Kit Recall: 1,870 Kits Recalled for OOS Dissolution Issue
Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
Sun Pharmaceutical Industries
Failed Dissolution